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D W Cox

Showing results (51-60 of 223) with videos related to

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Experimental Brain Research|January 1, 1988
Partial attenuation of dentate granule cell evoked activity by the alternative substrates, lactate and pyruvate: evidence for a postsynaptic actionD W Cox, H S Bachelard
Lancet (London, England)|July 22, 1998
Effect of treatment of Wilson's disease on natural history of haemochromatosisJ M Walshe, D W Cox
Trends in Genetics : TIG|July 1, 1994
Wilson disease and Menkes disease: new handles on heavy-metal transportP C Bull, D W Cox
Pediatric Clinics of North America|August 1, 1979
Genetic aspects of pediatric lung diseaseD W Cox, R C Talamo
Human Molecular Genetics|August 15, 2000
Copper-dependent trafficking of Wilson disease mutant ATP7B proteinsJ R Forbes, D W Cox
Genomics|June 1, 1993
Long range restriction mapping of 13q14.3 focused on the Wilson disease regionP C Bull, D W Cox
Genomics|September 1, 1994
Mapping of human immunoglobulin heavy chain variable gene segments outside the major IGH locusR F Wintle, D W Cox
Clinica Chimica Acta; International Journal of Clinical Chemistry|March 14, 1983
alpha 2-Macroglobulin in patients with obstructive lung disease, with and without alpha 1-antitrypsin deficiencyJ E Brissenden, D W Cox
Nucleic Acids Research|June 11, 1987
Bgl II polymorphism for the alpha 1-antitrypsin-related gene on chromosome 14D W Cox, S E Coulson
Lancet (London, England)|September 27, 1986
Restriction enzyme MaeIII for prenatal diagnosis of alpha 1-antitrypsin deficiencyD W Cox, G D Billingsley
Pageof 23

Showing results (51-60 of 223) with videos related to

Sort By:
Pageof 23
Experimental Brain Research|January 1, 1988
Partial attenuation of dentate granule cell evoked activity by the alternative substrates, lactate and pyruvate: evidence for a postsynaptic actionD W Cox, H S Bachelard
Lancet (London, England)|July 22, 1998
Effect of treatment of Wilson's disease on natural history of haemochromatosisJ M Walshe, D W Cox
Trends in Genetics : TIG|July 1, 1994
Wilson disease and Menkes disease: new handles on heavy-metal transportP C Bull, D W Cox
Pediatric Clinics of North America|August 1, 1979
Genetic aspects of pediatric lung diseaseD W Cox, R C Talamo
Human Molecular Genetics|August 15, 2000
Copper-dependent trafficking of Wilson disease mutant ATP7B proteinsJ R Forbes, D W Cox
Genomics|June 1, 1993
Long range restriction mapping of 13q14.3 focused on the Wilson disease regionP C Bull, D W Cox
Genomics|September 1, 1994
Mapping of human immunoglobulin heavy chain variable gene segments outside the major IGH locusR F Wintle, D W Cox
Clinica Chimica Acta; International Journal of Clinical Chemistry|March 14, 1983
alpha 2-Macroglobulin in patients with obstructive lung disease, with and without alpha 1-antitrypsin deficiencyJ E Brissenden, D W Cox
Nucleic Acids Research|June 11, 1987
Bgl II polymorphism for the alpha 1-antitrypsin-related gene on chromosome 14D W Cox, S E Coulson
Lancet (London, England)|September 27, 1986
Restriction enzyme MaeIII for prenatal diagnosis of alpha 1-antitrypsin deficiencyD W Cox, G D Billingsley
Pageof 23